Canonical Allele Identifier: CA898240530

Gene: PPARG

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12447383G>T , CM000665.2:g.12447383G>T	GRCh38
NC_000003.11:g.12488882G>T , CM000665.1:g.12488882G>T	GRCh37
NC_000003.10:g.12463882G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011533842.1:c.1271-23438G>T	XP_011532144.1:n.1271-23438G>T
XM_011533842.2:c.1271-23438G>T	XP_011532144.1:n.1271-23438G>T